Metabolic products of Phomopsis oblonga. Part 2. Phomopsolide A and B, tiglic esters of two 6-substituted 5,6-dihydro-5-hydroxypyran-2-ones
- 1 January 1985
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 4,p. 865-869
- https://doi.org/10.1039/p19850000865
Abstract
Phomopsolide A and B, two boring/feeding deterrents for elm bark beetles, produced in vitro by the fungus Phomopsis oblonga, are shown to be (5S,6S)-5,6-dihydro-6-(4-hydroxy-3-oxopent-1Z-enyl)-5-(2-methylbut-2E-enoyloxy)-2H-pyran-2-one and (5S,6S)-5,6-dihydro-6-[(3S,4S)-3,5-dihydroxypent-1E-enyl)-5-(2-methylbut-2E-enoyloxy)-2H-pyran-2-one, respectively. Another active compound, (–)-6-(4-hydroxy-3-oxopent-1E-enyl)-2H-pyran-2-one, was also isolated but is considered to be an artefact.This publication has 3 references indexed in Scilit:
- Metabolic products of Phomopsis oblonga. Part 1. 3a,5a,6,7,8,9,9a,9b-Octahydro-7,9b-dimethylnaphtho[1,2-c]furan-1(3H)-one (oblongolide)Journal of the Chemical Society, Perkin Transactions 1, 1985
- Synthesis and stereochemistry of 2-pyrone derivatives related to some fungal metabolitesCanadian Journal of Chemistry, 1978
- Circular Dichroism and Optical Rotatory Dispersion — Principles and Application to the Investigation of the Stereochemistry of Natural ProductsAngewandte Chemie International Edition in English, 1968